CQV Engineer - Pharma Validation, Early Career

AMARIS ACT PTE. LTD.; Singapore; On-site; SGD 40,000 - 65,000; Full time

Job summary

AMARIS ACT PTE. LTD. in Singapore seeks a junior CQV professional to support commissioning, qualification, and validation of pharmaceutical equipment and systems in a regulated environment.

You will prepare protocols, scripts, and reports; work with cross-functional teams; document deviations; and ensure GMP and data integrity. English fluency is required. Ideal candidates have 1–3 years of CQV experience in pharma, exposure to QC/production equipment or HVAC qualification, and a strong

Qualifications

• Bachelor's degree or higher in Pharmaceutical Science, Life Sciences, Chemical Engineering, Biomedical Engineering, Instrumentation, Automation, or related field.
• 1–3 years of experience in commissioning, qualification, or validation in pharma or a regulated environment.
• Experience with QC equipment, production equipment, or HVAC qualification.
• Knowledge or practical experience in computerized system validation.

Responsibilities

• Support commissioning, qualification, and validation activities for pharmaceutical equipment and systems.
• Prepare, execute, and review qualification protocols, test scripts, and reports.
• Support qualification of QC equipment, production equipment, HVAC systems, and related instrumentation.
• Contribute to computerized system validation activities associated with equipment and validation software.
• Perform testing and document results per approved procedures.
• Identify, document, and support deviation resolution during qualification activities.
• Ensure qualification documentation complies with quality, GMP, and data integrity requirements.
• Support performance qualification activities including process, cleaning, or single-use material qualification.
• Work with validation, engineering, quality, manufacturing, and QC teams.

Skills

CQV experience

GMP knowledge

Documentation protocols

Deviations handling

Process validation

Test scripts

Cross-functional collaboration

English fluency

Education

Bachelor's in Pharmaceutical Science or Life Sciences

Tools

QC equipment

HVAC qualification

Job description

AMARIS ACT PTE. LTD. in Singapore seeks a junior CQV professional to support commissioning, qualification, and validation of pharmaceutical equipment and systems in a regulated environment.

You will prepare protocols, scripts, and reports; work with cross-functional teams; document deviations; and ensure GMP and data integrity. English fluency is required. Ideal candidates have 1–3 years of CQV experience in pharma, exposure to QC/production equipment or HVAC qualification, and a strong